Canonical Allele Identifier: CA2275549601

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75518826A= , CM000679.2:g.75518826A=	GRCh38
NC_000017.10:g.73514907A= , CM000679.1:g.73514907A=	GRCh37
NC_000017.9:g.71026502A=	NCBI36
NG_013041.1:g.7299A=
NG_033152.1:g.1758T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.469-169A= MANE Select	ENSP00000327487.6:n.469-169A=
ENST00000434205.8:c.166-169A=	ENSP00000406559.4:n.166-169A=
ENST00000545228.3:c.469-169A=	ENSP00000438169.3:n.469-169A=
ENST00000579449.2:n.268-169A=
ENST00000580013.6:n.478-169A=
ENST00000583818.2:c.469-169A=	ENSP00000461928.2:n.469-169A=
ENST00000679370.1:n.856-169A=
ENST00000679429.1:c.469-177A=	ENSP00000505403.1:n.469-177A=
ENST00000679443.1:n.344-169A=
ENST00000679782.1:c.469-169A=	ENSP00000505995.1:n.469-169A=
ENST00000679919.1:n.344-169A=
ENST00000679928.1:c.469-169A=	ENSP00000506071.1:n.469-169A=
ENST00000680528.1:n.494-169A=
ENST00000680999.1:c.469-169A=	ENSP00000504984.1:n.469-169A=
ENST00000681282.1:c.469-169A=	ENSP00000506339.1:n.469-169A=
ENST00000333213.10:c.469-169A=	ENSP00000327487.6:n.469-169A=
ENST00000434205.7:c.166-169A=	ENSP00000406559.3:n.166-169A=
ENST00000578415.1:c.429-169A=
ENST00000580013.5:n.494-177A=
ENST00000583173.5:c.304-169A=	ENSP00000463619.1:n.304-169A=
ENST00000583818.1:c.364-169A=	ENSP00000461928.1:n.364-169A=
NM_207346.2:c.469-169A=	NP_997229.2:n.469-169A=
XM_005257229.2:c.469-169A=	XP_005257286.1:n.469-169A=
XM_006721821.2:c.166-169A=	XP_006721884.1:n.166-169A=
XM_011524616.1:c.469-169A=	XP_011522918.1:n.469-169A=
XM_011524617.1:c.469-169A=	XP_011522919.1:n.469-169A=
XM_011524618.1:c.469-169A=	XP_011522920.1:n.469-169A=
XR_243646.2:n.499-169A=
XM_005257229.4:c.469-169A=	XP_005257286.1:n.469-169A=
XR_243646.4:n.505-169A=
NM_207346.3:c.469-169A= MANE Select	NP_997229.2:n.469-169A=